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Detecting Diabetes Sooner With a Risk Survey for the Family Doctor:Comparing Internet and Traditional Methods of Communication for Patients and Doctors

Not Applicable
Conditions
Diabetes
Interventions
Other: CANRISK (Canadian Diabetes Association Assessment)
Registration Number
NCT01529918
Lead Sponsor
McMaster University
Brief Summary

This pilot RCT study aims to develop and evaluate the uptake, feasibility, and potential value of a strategy for web-diabetes risk assessment versus paper-based methods in an undiagnosed diabetes population over 40 years of age from all listed FHT provided through an electronic medical record database. Following randomization, intervention participants will have the option to decide to use web-based self-screening and the control group will receive only a paper-based method. There will be two options for web-based screening; one involves completion of the CAN-RISK screening tool as part of a personal health record self-management program (MyOscar) versus a one off online risk-assessment. The intervention and control group will be compared with respect to risk-assessment uptake. Educational sessions and further assessment of diabetes conducted by the clinical health care team will be offered to all participants who scored a high risk of diabetes in accordance with the CAN-RISK results. Actual numbers of diabetes cases in those with a high risk score will be compared between the intervention and control groups as well as compared to the usual method of diabetes screening in a randomly chosen non-identifiable sample from the same clinical setting in the same one year period. The assessment of patient acceptability in feasibility of the implementation of the self-screening tool will be accomplished through surveys designed to be completed by patients and staff.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
2000
Inclusion Criteria
  • Patients aged 40 and over who did not have diagnosis of diabetes and no previous use of personal health record (MyOscar)
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Exclusion Criteria
  • People with diabetes, and those who are already registered as MyOSCAR (personal e-health record) users
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
web-intervention groupCANRISK (Canadian Diabetes Association Assessment)Participants will receive access to the CAN-RISK (Canadian Diabetes Risk Assessment) questionnaire either via personal patient electronic health record or an online version
paper-based groupCANRISK (Canadian Diabetes Association Assessment)Participants allocated to paper-based will receive the CAN-RISK questionnaire for diabetes risk-assessment via paper-based
Primary Outcome Measures
NameTimeMethod
Patient's uptake and preferences1 year

Numbers of patients participating in the self risk-assessment, and a comparison of paper versus web-based technologies will be collected.

* Demographics of the 2 groups will be compared.

* A user-satisfaction survey will assess patients' perceptions of the technologies. Use of necessary qualitative techniques can be considered as well.

Secondary Outcome Measures
NameTimeMethod
The comparison of yield of actual diabetes detected from those who have high risk at self risk-assessment, compared to the usual diabetes detection rate in a random sample from the practice within a one year period.1 year
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